| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:75510945-75511190 | Common:1; Rare:50 | ||||
| chr12:75511569-75511715 | Rare:53 | ||||
| chr12:76031278-76031374 | Rare:29 | ||||
| chr12:76031416-76031505 | Rare:33 | ||||
| chr12:76031507-76032017 | Common:1; Rare:149 | ||||
| chr12:76032191-76032513 | Common:2; Rare:67 | ||||
| chr12:76083856-76084207 | Common:1; Rare:92 | ||||
| chr12:76084478-76085142 | Common:7; Rare:185 | ||||
| chr12:76348067-76348225 | Rare:45; Clinvar (pathogenic):2 | ||||
| chr12:76348297-76348620 | Common:2; Rare:110; Clinvar:4; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr12:76422741-76423092 | Common:2; Rare:74 | ||||
| chr12:76423109-76423355 | Common:1; Rare:49 | ||||
| chr12:76559020-76559267 | Common:2; Rare:45 | ||||
| chr12:76559361-76559401 | Rare:5 | ||||
| chr12:76559631-76560006 | Rare:131 |